{"id":1792,"date":"2016-11-04T10:00:59","date_gmt":"2016-11-04T01:00:59","guid":{"rendered":"https:\/\/www.hamarichemicals.com\/eng\/?page_id=1792"},"modified":"2026-01-26T14:54:48","modified_gmt":"2026-01-26T05:54:48","slug":"publication-list","status":"publish","type":"page","link":"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/","title":{"rendered":"Scientific Publications"},"content":{"rendered":"<div id=\"lowR\" style=\"border-radius: 0.5rem;\">\n<div id=\"lowRin\" class=\"tec01\">\n<h1>Hamari&#8217;s Scientific Publications<\/h1>\n<p><strong>Contribution to the Scientific Community.<\/strong> Hamari is a trend setter when it comes to developing new technology and applying its unique technology for commercial purposes. Contribution to the scientific community makes Hamari stands out from its competitors.<\/p>\n<h3>Featured Publications<\/h3>\n<ul style=\"padding-left: 1rem;\">\n<li style=\"padding: 0.4rem; background-color: #edfac7;\"><strong>Chemical dynamic kinetic resolution and <em>S\/R<\/em> interconversion of unprotected \u03b1-amino acids. <\/strong><em>Angew. Chem. Int. Ed.<\/em> <strong>2014<\/strong>, <em>53<\/em>, 12214\u201312217. DOI: 10.1002\/anie.201407944<\/li>\n<li style=\"margin-top: 0.4rem; padding: 0.4rem; background-color: #edfac7;\"><strong>Recyclable ligands for the non-enzymatic dynamic kinetic resolution of challenging \u03b1-amino acids. <\/strong><em>Angew. Chem. Int. Ed.<\/em> <strong>2015<\/strong>, <em>54<\/em>, 12918\u201312922. DOI: 10.1002\/anie.201507273<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p class=\"mB10\"><strong>Catering to your needs.<\/strong> If you require chemical synthesis for your scientific research, do not hesitate and contact Hamari for collaborative work. Together we can accelerate your research and benefit mankind!<\/p>\n<h3>Selected List of Published Research and Review Articles and Patents<\/h3>\n<p>The following is a selected list of peer-reviewed research articles authored by Hamari Chemicals, Ltd.<\/p>\n<ol class=\"jeff2 f10px\">\n<li><strong>Identification of Tamsulosin-Dimeric Impurity, Leading to the Efficient Manufacturing Process of the Active Pharmaceutical Ingredient.<\/strong> <em>Org. Process Res. Dev.<\/em> <strong>2025<\/strong>, DOI:10.1021\/acs.oprd.5c00211<\/li>\n<li><strong>Development of an Innovative Three-Component Optical Resolution and a Flow Chemistry Process for (<em>R<\/em>)-Troloxamide Quinone (EPI-589).<\/strong> <em>Org. Process Res. Dev.<\/em> <strong>2025<\/strong>,  <em>29<\/em>, 1197-1021. DOI:10.1021\/acs.oprd.4c00540<\/li>\n<li><strong>HAMARI\u2019S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS.<\/strong> <em>Ukr. Chem. J.<\/em> <strong>2024<\/strong>, <em>90<\/em>, 88-134. DOI: 10.33609\/2708-129X.90.10.2024.88-134<\/li>\n<li><strong>Dynamic Thermodynamic Resolution of Unprotected Amino Acids Using Ni(II) Chiral Schiff Bases.<\/strong> <em>Eur. J. Org. Chem.<\/em> <strong>2024<\/strong>, <em>27<\/em>, e202400417. DOI: 10.1002\/ejoc.202400417<\/li>\n<li><strong>Rapid and efficient syntheses of tryptophans using a continuous-flow quaternization\u2013substitution reaction of gramines with a chiral nucleophilic glycine equivalent.<\/strong> <em>Org. Biomol. Chem.<\/em> <strong>2022<\/strong>, <em>20<\/em>, 8331-8340. DOI: 10.1039\/d2ob01682f<\/li>\n<li><strong>Aldol addition-cyclization reaction cascade on a platform of chiral Ni(II) complex of glycine Schiff base.<\/strong> <em>Ukr. Bioorg. Acta<\/em> <strong>2021<\/strong>, <em>16<\/em>, 3-9. DOI: 10.15407\/bioorganica2021.01.003<\/li>\n<li><strong>Asymmetric synthesis of (<em>S<\/em>)-\u03b1-(octyl)glycine via alkylation of Ni(II) complex of chiral glycine Schiff base.<\/strong> <em>Chirality<\/em> <strong>2020<\/strong>, <em>32<\/em>, 1354-1360. DOI: 10.1002\/chir.23281<\/li>\n<li><strong>Michael addition reactions of chiral glycine Schiff base Ni(II)-complex with 1-(1-phenylsulfonyl)benzene.<\/strong> <em>Chirality<\/em> <strong>2020<\/strong>, <em>32<\/em>, 885-893. DOI: 10.1002\/chir.23203<\/li>\n<li><strong>Asymmetric Synthesis of 4,4\u2010(Difluoro)glutamic Acid via Chiral Ni(II)\u2010Complexes of Dehydroalanine Schiff Bases. Effect of the Chiral Ligands Structure on the Stereochemical Outcome.<\/strong> <em>ChemistryOpen<\/em> <strong>2020<\/strong>, <em>9<\/em>, 93-96. DOI: 10.1002\/open.201900343<\/li>\n<li><strong>Large-Scale Synthesis of the Glycine Schiff Base Ni(II) Complex Derived from (<em>S<\/em>)- and (<em>R<\/em>)-<em>N<\/em>-(2-Benzoyl-4-chlorophenyl)-1-[(3,4-dichlorophenyl)methyl]-2-pyrrolidinecarboxamide.<\/strong> <em>Org. Process Res. Dev.<\/em> <strong>2020<\/strong>,  <em>24<\/em>, 294-300. DOI: 10.1021\/acs.oprd.9b00399<\/li>\n<li><strong>Development of Hamari Ligands for Practical Asymmetric Synthesis of Tailor-Made Amino Acids.<\/strong> <em>ACS Omega<\/em> <strong>2019<\/strong>, <em>4<\/em>, 18942-18947. DOI: 10.1021\/acsomega.9b02940<\/li>\n<li><strong>Practical Method for Preparation of (<em>S<\/em>)-2-Amino-5,5,5-trifluoropentanoic Acid via Dynamic Kinetic Resolution.<\/strong> <em>ACS Omega<\/em> <strong>2019<\/strong>, <em>4<\/em>, 11844-11851. DOI: 10.1021\/acsomega.9b01537<\/li>\n<li><strong>Large\u2010Scale Asymmetric Synthesis of Fmoc\u2010(<em>S<\/em>)\u20102\u2010Amino\u20106,6,6\u2010Trifluorohexanoic Acid.<\/strong> <em>ChemistryOpen<\/em> <strong>2019<\/strong>, <em>8<\/em>, 701-704. DOI: 10.1002\/open.201900131<\/li>\n<li><strong>Optical Resolution of Rimantadine. <\/strong><em>Molecules<\/em> <strong>2019<\/strong>, <em>24<\/em>, 1828. DOI: 10.3390\/molecules24091828<\/li>\n<li><strong>Convenient Asymmetric Synthesis of Fmoc-(<em>S<\/em>)-6,6,6-Trifluoro-Norleucine. <\/strong><em>Symmetry <\/em> <strong>2019<\/strong>, <em>11<\/em>, 578. DOI: 10.3390\/sym11040578<\/li>\n<li><strong>Expedient Asymmetric Synthesis of (<em>S<\/em>)\u20112-Amino-4,4,4-trifluorobutanoic Acid <em>via<\/em> Alkylation of Chiral Nucleophilic Glycine Equivalent. <\/strong><em>Org. Process Res. Dev. <\/em> <strong>2019<\/strong>, <em>23<\/em>, 629\u2013634. DOI: 10.1021\/acs.oprd.8b00404<\/li>\n<li><strong>Large Scale Synthesis of Chiral (3<em>Z<\/em>,5<em>Z<\/em>)\u20112,7-Dihydro\u20111<em>H<\/em>\u2011azepine-Derived Hamari Ligand for General Asymmetric Synthesis of Tailor-Made Amino Acids. <\/strong><em>Org. Process Res. Dev. <\/em> <strong>2019<\/strong>, <em>23<\/em>, 619\u2013628. DOI: 10.1021\/acs.oprd.8b00406<\/li>\n<\/ol>\n<p class=\"mT20\">The following is a selected review article authored by Hamari Chemicals, Ltd.<\/p>\n<ol class=\"jeff2 f10px\">\n<li><strong>Tailor-made amino acids in the design of small-molecule blockbuster drugs. <\/strong> <em>Eur. J. Med. Chem.<\/em> <strong>2021<\/strong>, <em>220<\/em>, 113448. DOI: 10.1016\/j.ejmech.2021.113448<\/li>\n<li><strong>Tailor-made amino acid-derived pharmaceuticals approved by the FDA in 2019. <\/strong><em>Amino Acids<\/em> <strong>2020<\/strong>, <em>52<\/em>, 1227-1261. DOI: 10.1007\/s00726-020-02887-4<\/li>\n<li><strong>Cyclic tailor-made amino acids in the design of modern pharmaceuticals. <\/strong><em>Eur. J. Med. Chem.<\/em> <strong>2020<\/strong>, <em>208<\/em>, 112736. DOI: 10.1016\/j.ejmech.2020.112736<\/li>\n<li><strong>Tailor-made amino acids and fluorinated motifs as prominent traits in modern pharmaceuticals. <\/strong><em>Chem. Eur. J.<\/em> <strong>2020<\/strong>, <em>26<\/em>, 11349-11390. <span style=\"color: #ff0000\">[<em>Reviews Showcase<\/em>]<\/span> DOI: 10.1002\/chem.202085061<\/li>\n<li><strong>Applications of fluorine-containing amino acids for drug design. <\/strong><em>Eur. J. Med. Chem.<\/em> <strong>2020<\/strong>, <em>186<\/em>, 111826. DOI: 10.1016\/j.ejmech.2019.111826<\/li>\n<li><strong>The second-generation of highly potent Hepatitis C virus (HCV) NS3\/4A protease inhibitors: Evolutionary design based on tailor-made amino acids, synthesis and major features of bio-activity.\u00a0<\/strong><em>Curr. Pharm. Des. <\/em><strong>2017<\/strong>, <em>23<\/em>, 4493\u20134554. DOI: 10.2174\/1381612823666170522122424<\/li>\n<li><strong>New routes to tailor-made amino acids.<\/strong> <em>Speciality Chemicals Magazine<\/em> <strong>March 2016<\/strong>, <em>36<\/em>, 42\u201343. Corpus ID: 90106437<\/li>\n<li><strong>Next generation of fluorine-containing pharmaceuticals, compounds currently in Phase II\u2013III clinical trials of major pharmaceutical companies: New structural trends and therapeutic areas.\u00a0<\/strong><em>Chem. Rev.<\/em> <strong>2016<\/strong>, <em>116<\/em>, 422\u2013518. DOI: 10.1021\/acs.chemrev.5b00392<\/li>\n<li><strong>Small-molecule therapeutics for Ebola virus (EBOV) disease treatment.\u00a0<\/strong><em>Eur. J. Org. Chem.<\/em> <strong>2016<\/strong>, <em>1<\/em>, 8\u201316. DOI: 10.1002\/ejoc.201501158<\/li>\n<li><strong>Tailor-made \u03b1-amino acids in the pharmaceutical industry: Synthetic approaches to (1<em>R<\/em>,2<em>S<\/em>)-1-Amino-2-vinylcyclopropane-1-carboxylic acid (Vinyl-ACCA).\u00a0<\/strong><em>Eur. J. Org. Chem.<\/em> <strong>2016<\/strong>, <em>16<\/em>, 2757\u20132774. DOI: 10.1002\/ejoc.201600112<\/li>\n<li><strong>Recent advances in the trifluoromethylation methodology and new CF<sub>3<\/sub>-containing drugs.\u00a0<\/strong><em>J. Fluorine Chem.<\/em> <strong>2014<\/strong>, <em>167<\/em>, 37\u201354. DOI: 10.1016\/j.jfluchem.2014.06.026<\/li>\n<li><strong>Synthesis of fluorine-containing \u03b1-amino acids in enantiomerically pure form <em>via<\/em> homologation of Ni(II) complexes of glycine and alanine Schiff bases.\u00a0<\/strong><em>J. Fluorine Chem.<\/em> <strong>2013<\/strong>, <em>155<\/em>, 21\u201338. DOI: 10.1016\/j.jfluchem.2013.06.004<\/li>\n<\/ol>\n<p class=\"mT20\">The following is a selected list of patents by Hamari Chemicals, Ltd.<\/p>\n<ol class=\"jeff2 f10px\">\n<li><strong>METHOD FOR PRODUCING PEPTIDE.<\/strong> WO2018181679.<\/li>\n<li><strong>METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL.<\/strong> WO2013061999.<\/li>\n<li><strong>METHOD FOR PRODUCING OPTICALLY ACTIVE TETRAHYDROQUINOLINE.<\/strong> WO2013011930.<\/li>\n<li><strong>METHOD FOR PRODUCING FINE POWDER OF LOXOPROFEN SODIUM DIHYDRATE FOR PHARMACEUTICAL PREPARATIONS.<\/strong> WO2012137667.<\/li>\n<li><strong> METHOD FOR PRODUCING OPTICALLY ACTIVE AMINE.<\/strong> WO2009005024.<\/li>\n<\/ol>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Hamari&#8217;s Scientific Publications Contribution to the Scientific Community. Hamari is a trend setter when it comes to developing new technology and applying its unique technology for commercial purposes. Contribution to the scientific community makes Hamari stands out from its competitors. Featured Publications Chemical dynamic kinetic resolution and S\/R interconversion of unprotected \u03b1-amino acids. Angew. Chem. Int. Ed. 2014, 53, 12214\u201312217. DOI: 10.1002\/anie.201407944 Recyclable ligands for the non-enzymatic dynamic kinetic resolution of challenging \u03b1-amino acids. Angew. Chem. Int. Ed. 2015, 54, 12918\u201312922. DOI: 10.1002\/anie.201507273 &nbsp; Catering to your needs. If you require chemical synthesis for your scientific research, do not hesitate and contact Hamari for collaborative work. Together we can accelerate your research and benefit mankind! Selected List of Published Research and Review Articles and Patents The following is a selected list of peer-reviewed research articles authored by Hamari Chemicals, Ltd. Identification of Tamsulosin-Dimeric Impurity, Leading to the Efficient Manufacturing Process of the Active Pharmaceutical Ingredient. Org. Process Res. Dev. 2025, DOI:10.1021\/acs.oprd.5c00211 Development of an Innovative Three-Component Optical Resolution and a Flow Chemistry Process for (R)-Troloxamide Quinone (EPI-589). Org. Process Res. Dev. 2025, 29, 1197-1021. DOI:10.1021\/acs.oprd.4c00540 HAMARI\u2019S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS. Ukr. Chem. J. 2024, 90, 88-134. DOI: 10.33609\/2708-129X.90.10.2024.88-134 Dynamic Thermodynamic Resolution of Unprotected Amino Acids Using Ni(II) Chiral Schiff Bases. Eur. J. Org. Chem. 2024, 27, e202400417. DOI: 10.1002\/ejoc.202400417 Rapid and efficient syntheses of tryptophans using a continuous-flow quaternization\u2013substitution reaction of gramines with a chiral nucleophilic glycine equivalent. Org. Biomol. Chem. 2022, 20, 8331-8340. DOI: 10.1039\/d2ob01682f Aldol addition-cyclization reaction cascade on a platform of chiral Ni(II) complex of glycine Schiff base. Ukr. Bioorg. Acta 2021, 16, 3-9. DOI: 10.15407\/bioorganica2021.01.003 Asymmetric synthesis of (S)-\u03b1-(octyl)glycine via alkylation of Ni(II) complex of chiral glycine Schiff base. Chirality 2020, 32, 1354-1360. DOI: 10.1002\/chir.23281 Michael addition reactions of chiral glycine<a class=\"read\" href=\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/\">[&#8230;Continue Reading]<\/a><\/p>\n","protected":false},"author":4,"featured_media":0,"parent":13,"menu_order":8,"comment_status":"closed","ping_status":"closed","template":"page-technology.php","meta":{"footnotes":""},"class_list":["post-1792","page","type-page","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Scientific Publications - Hamari Chemicals, Ltd.<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Scientific Publications - Hamari Chemicals, Ltd.\" \/>\n<meta property=\"og:description\" content=\"Hamari&#8217;s Scientific Publications Contribution to the Scientific Community. Hamari is a trend setter when it comes to developing new technology and applying its unique technology for commercial purposes. Contribution to the scientific community makes Hamari stands out from its competitors. Featured Publications Chemical dynamic kinetic resolution and S\/R interconversion of unprotected \u03b1-amino acids. Angew. Chem. Int. Ed. 2014, 53, 12214\u201312217. DOI: 10.1002\/anie.201407944 Recyclable ligands for the non-enzymatic dynamic kinetic resolution of challenging \u03b1-amino acids. Angew. Chem. Int. Ed. 2015, 54, 12918\u201312922. DOI: 10.1002\/anie.201507273 &nbsp; Catering to your needs. If you require chemical synthesis for your scientific research, do not hesitate and contact Hamari for collaborative work. Together we can accelerate your research and benefit mankind! Selected List of Published Research and Review Articles and Patents The following is a selected list of peer-reviewed research articles authored by Hamari Chemicals, Ltd. Identification of Tamsulosin-Dimeric Impurity, Leading to the Efficient Manufacturing Process of the Active Pharmaceutical Ingredient. Org. Process Res. Dev. 2025, DOI:10.1021\/acs.oprd.5c00211 Development of an Innovative Three-Component Optical Resolution and a Flow Chemistry Process for (R)-Troloxamide Quinone (EPI-589). Org. Process Res. Dev. 2025, 29, 1197-1021. DOI:10.1021\/acs.oprd.4c00540 HAMARI\u2019S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS. Ukr. Chem. J. 2024, 90, 88-134. DOI: 10.33609\/2708-129X.90.10.2024.88-134 Dynamic Thermodynamic Resolution of Unprotected Amino Acids Using Ni(II) Chiral Schiff Bases. Eur. J. Org. Chem. 2024, 27, e202400417. DOI: 10.1002\/ejoc.202400417 Rapid and efficient syntheses of tryptophans using a continuous-flow quaternization\u2013substitution reaction of gramines with a chiral nucleophilic glycine equivalent. Org. Biomol. Chem. 2022, 20, 8331-8340. DOI: 10.1039\/d2ob01682f Aldol addition-cyclization reaction cascade on a platform of chiral Ni(II) complex of glycine Schiff base. Ukr. Bioorg. Acta 2021, 16, 3-9. DOI: 10.15407\/bioorganica2021.01.003 Asymmetric synthesis of (S)-\u03b1-(octyl)glycine via alkylation of Ni(II) complex of chiral glycine Schiff base. Chirality 2020, 32, 1354-1360. DOI: 10.1002\/chir.23281 Michael addition reactions of chiral glycine[...Continue Reading]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/\" \/>\n<meta property=\"og:site_name\" content=\"Hamari Chemicals, Ltd.\" \/>\n<meta property=\"article:modified_time\" content=\"2026-01-26T05:54:48+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"4 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/\",\"url\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/\",\"name\":\"Scientific Publications - Hamari Chemicals, Ltd.\",\"isPartOf\":{\"@id\":\"https:\/\/www.hamarichemicals.com\/eng\/#website\"},\"datePublished\":\"2016-11-04T01:00:59+00:00\",\"dateModified\":\"2026-01-26T05:54:48+00:00\",\"breadcrumb\":{\"@id\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"\u30db\u30fc\u30e0\",\"item\":\"https:\/\/www.hamarichemicals.com\/eng\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Technology\",\"item\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"Scientific Publications\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.hamarichemicals.com\/eng\/#website\",\"url\":\"https:\/\/www.hamarichemicals.com\/eng\/\",\"name\":\"Hamari Chemicals, Ltd.\",\"description\":\"Hamari Chemicals, Ltd.&#039;s Website\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.hamarichemicals.com\/eng\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Scientific Publications - Hamari Chemicals, Ltd.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/","og_locale":"en_US","og_type":"article","og_title":"Scientific Publications - Hamari Chemicals, Ltd.","og_description":"Hamari&#8217;s Scientific Publications Contribution to the Scientific Community. Hamari is a trend setter when it comes to developing new technology and applying its unique technology for commercial purposes. Contribution to the scientific community makes Hamari stands out from its competitors. Featured Publications Chemical dynamic kinetic resolution and S\/R interconversion of unprotected \u03b1-amino acids. Angew. Chem. Int. Ed. 2014, 53, 12214\u201312217. DOI: 10.1002\/anie.201407944 Recyclable ligands for the non-enzymatic dynamic kinetic resolution of challenging \u03b1-amino acids. Angew. Chem. Int. Ed. 2015, 54, 12918\u201312922. DOI: 10.1002\/anie.201507273 &nbsp; Catering to your needs. If you require chemical synthesis for your scientific research, do not hesitate and contact Hamari for collaborative work. Together we can accelerate your research and benefit mankind! Selected List of Published Research and Review Articles and Patents The following is a selected list of peer-reviewed research articles authored by Hamari Chemicals, Ltd. Identification of Tamsulosin-Dimeric Impurity, Leading to the Efficient Manufacturing Process of the Active Pharmaceutical Ingredient. Org. Process Res. Dev. 2025, DOI:10.1021\/acs.oprd.5c00211 Development of an Innovative Three-Component Optical Resolution and a Flow Chemistry Process for (R)-Troloxamide Quinone (EPI-589). Org. Process Res. Dev. 2025, 29, 1197-1021. DOI:10.1021\/acs.oprd.4c00540 HAMARI\u2019S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS. Ukr. Chem. J. 2024, 90, 88-134. DOI: 10.33609\/2708-129X.90.10.2024.88-134 Dynamic Thermodynamic Resolution of Unprotected Amino Acids Using Ni(II) Chiral Schiff Bases. Eur. J. Org. Chem. 2024, 27, e202400417. DOI: 10.1002\/ejoc.202400417 Rapid and efficient syntheses of tryptophans using a continuous-flow quaternization\u2013substitution reaction of gramines with a chiral nucleophilic glycine equivalent. Org. Biomol. Chem. 2022, 20, 8331-8340. DOI: 10.1039\/d2ob01682f Aldol addition-cyclization reaction cascade on a platform of chiral Ni(II) complex of glycine Schiff base. Ukr. Bioorg. Acta 2021, 16, 3-9. DOI: 10.15407\/bioorganica2021.01.003 Asymmetric synthesis of (S)-\u03b1-(octyl)glycine via alkylation of Ni(II) complex of chiral glycine Schiff base. Chirality 2020, 32, 1354-1360. 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